| NDC Code: |
51079-779 |
| Proprietary Name: |
Hydrocodone Bitartrate And Acetaminophen |
| Suffix: |
|
| Non-Proprietary Name: |
Hydrocodone Bitartrate And Acetaminophen |
| Dosage Form: |
TABLET |
| Method: |
ORAL |
| Original Marketing Date: |
08-11-2011 |
| Category Name: |
ANDA |
| Application Number: |
ANDA040355 |
| Labeler: |
UDL LABORATORIES, INC. |
| Substance Name: |
ACETAMINOPHEN; HYDROCODONE BITARTRATE |
| Active Numerator Strength: |
325; 10 |
| Active Ingredient Unit: |
mg/1; mg/1 |
| Pharm Classes: |
Opioid Agonist [EPC],Opioid Agonists [MoA] |
| DEA Schedule: |
CIII |
